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在成纤维细胞培养物中,磷脂的代谢有节律地振荡,并受生物钟蛋白周期蛋白1调控。

The metabolism of phospholipids oscillates rhythmically in cultures of fibroblasts and is regulated by the clock protein PERIOD 1.

作者信息

Marquez Sebastian, Crespo Pilar, Carlini Valeria, Garbarino-Pico Eduardo, Baler Ruben, Caputto Beatriz L, Guido Mario E

机构信息

CIQUIBIC, Departamento de Química Biológica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000 Córdoba, Argentina.

出版信息

FASEB J. 2004 Mar;18(3):519-21. doi: 10.1096/fj.03-0417fje. Epub 2004 Jan 8.

Abstract

The mammalian circadian timing system is composed of countless cell oscillators distributed throughout the body and central pacemakers regulating temporal physiology and behavior. Peripheral clocks display circadian rhythms in gene expression both in vivo and in culture. We examined the biosynthesis of phospholipids as well as the expression of the clock gene period 1 (Per1) and its potential involvement in the regulation of the phospholipid metabolism in cultured quiescent NIH 3T3 cells synchronized by a 2 h serum shock. A 30 min pulse of radiolabeled precursor was given at phases ranging from 0.5 to 62 h after serum treatment. We observed a daily rhythm in the phospholipid labeling that persisted at least for two cycles, with levels significantly decreasing 29 and 58 h after treatment. Per1 expression exhibited a rapid and transient induction and a daily rhythmicity in antiphase to the lipid labeling. After Per1 expression knockdown, the rhythm of phospholipid labeling was lost. Furthermore, in cultures of CLOCK mutant fibroblasts--cells with a clock mechanism impairment--PER1 was equally expressed at all times examined and the phospholipid labeling did not oscillate. The results demonstrate that the biosynthesis of phospholipids oscillates daily in cultured fibroblasts by an endogenous clock mechanism involving Per1 expression.

摘要

哺乳动物的昼夜节律计时系统由遍布全身的无数细胞振荡器和调节时间生理和行为的中央起搏器组成。外周生物钟在体内和体外培养中均显示出基因表达的昼夜节律。我们研究了磷脂的生物合成以及时钟基因周期蛋白1(Per1)的表达,及其在通过2小时血清休克同步化的培养静止NIH 3T3细胞中对磷脂代谢调节的潜在参与。在血清处理后的0.5至62小时的不同阶段给予30分钟的放射性标记前体脉冲。我们观察到磷脂标记存在每日节律,至少持续两个周期,处理后29小时和58小时水平显著下降。Per1表达表现出快速且短暂的诱导,并且与脂质标记呈反相的每日节律。Per1表达敲低后,磷脂标记的节律消失。此外,在CLOCK突变成纤维细胞(时钟机制受损的细胞)培养物中,PER1在所有检测时间均等量表达,并且磷脂标记不发生振荡。结果表明,通过涉及Per1表达的内源性时钟机制,培养的成纤维细胞中磷脂的生物合成每日振荡。

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